Effects of genetic variability of Mycobacterium tuberculosis strains on the presentation of disease
The nature of the variability in the clinical and epidemiological consequences of Mycobacterium tuberculosis infection remains poorly understood. Environmental and host factors that contribute to the outcome of infection and disease presentation are well recognised, but the role of bacterial factors...
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description | The nature of the variability in the clinical and epidemiological consequences of Mycobacterium tuberculosis infection remains poorly understood. Environmental and host factors that contribute to the outcome of infection and disease presentation are well recognised, but the role of bacterial factors has been more elusive. The rapid increase in the understanding of the molecular basis of M tuberculosis over the past decades has revived research into its pathogenesis. DNA fingerprinting techniques have been used to distinguish between strains of M tuberculosis, and efforts to characterise the strains present within populations have led to increased understanding of their global distribution. This research has shown that in certain areas a small number of strains are causing a disproportionate number of cases of the disease. The sequencing of the complete genome of M tuberculosis has accelerated the development of molecular techniques to differentiate strains according to their genetic polymorphisms. Investigation into the reasons why some strains are predominant by genetic strain-typing techniques may clarify which bacterial factors contribute to disease. This knowledge has the potential to influence control and prevention strategies for tuberculosis in the future. However, there are still limitations in these techniques and their results. This review discusses molecular epidemiology and genetic studies, and their contribution to the understanding of the links between genotypic and phenotypic characteristics of M tuberculosis strains. |
doi_str_mv | 10.1016/S1473-3099(05)01310-1 |
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Environmental and host factors that contribute to the outcome of infection and disease presentation are well recognised, but the role of bacterial factors has been more elusive. The rapid increase in the understanding of the molecular basis of M tuberculosis over the past decades has revived research into its pathogenesis. DNA fingerprinting techniques have been used to distinguish between strains of M tuberculosis, and efforts to characterise the strains present within populations have led to increased understanding of their global distribution. This research has shown that in certain areas a small number of strains are causing a disproportionate number of cases of the disease. The sequencing of the complete genome of M tuberculosis has accelerated the development of molecular techniques to differentiate strains according to their genetic polymorphisms. Investigation into the reasons why some strains are predominant by genetic strain-typing techniques may clarify which bacterial factors contribute to disease. This knowledge has the potential to influence control and prevention strategies for tuberculosis in the future. However, there are still limitations in these techniques and their results. This review discusses molecular epidemiology and genetic studies, and their contribution to the understanding of the links between genotypic and phenotypic characteristics of M tuberculosis strains.</description><identifier>ISSN: 1473-3099</identifier><identifier>EISSN: 1474-4457</identifier><identifier>DOI: 10.1016/S1473-3099(05)01310-1</identifier><identifier>PMID: 15766652</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Animals ; Antitubercular Agents - therapeutic use ; Bacterial diseases ; Biological and medical sciences ; Deoxyribonucleic acid ; Disease ; Disease control ; DNA ; DNA Fingerprinting ; Drug resistance ; Epidemiology ; Gene sequencing ; Genetic fingerprinting ; Genetic variability ; Genetic Variation ; Genomes ; Genomics ; Human bacterial diseases ; Humans ; Infections ; Infectious diseases ; Medical sciences ; Mice ; Molecular chains ; Molecular Epidemiology ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - classification ; Mycobacterium tuberculosis - drug effects ; Mycobacterium tuberculosis - genetics ; Pathogenesis ; Phenotypes ; Phylogenetics ; Polymerase Chain Reaction ; Polymorphism, Restriction Fragment Length ; Population Surveillance - methods ; Strains (organisms) ; Tuberculosis ; Tuberculosis and atypical mycobacterial infections ; Tuberculosis, Multidrug-Resistant - drug therapy ; Tuberculosis, Multidrug-Resistant - genetics ; Tuberculosis, Multidrug-Resistant - transmission</subject><ispartof>The Lancet infectious diseases, 2005-03, Vol.5 (3), p.174-183</ispartof><rights>2005 Elsevier Ltd</rights><rights>2005 INIST-CNRS</rights><rights>Copyright Elsevier Limited Mar 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c500t-da87282a4688219ba83b3c7719a297f9a8ff68cb20fa2b1c0af66adc607ef2e3</citedby><cites>FETCH-LOGICAL-c500t-da87282a4688219ba83b3c7719a297f9a8ff68cb20fa2b1c0af66adc607ef2e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2069921111?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,64361,64363,64365,65309,72215</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16526974$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15766652$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Malik, Aeesha NJ</creatorcontrib><creatorcontrib>Godfrey-Faussett, Peter</creatorcontrib><title>Effects of genetic variability of Mycobacterium tuberculosis strains on the presentation of disease</title><title>The Lancet infectious diseases</title><addtitle>Lancet Infect Dis</addtitle><description>The nature of the variability in the clinical and epidemiological consequences of Mycobacterium tuberculosis infection remains poorly understood. Environmental and host factors that contribute to the outcome of infection and disease presentation are well recognised, but the role of bacterial factors has been more elusive. The rapid increase in the understanding of the molecular basis of M tuberculosis over the past decades has revived research into its pathogenesis. DNA fingerprinting techniques have been used to distinguish between strains of M tuberculosis, and efforts to characterise the strains present within populations have led to increased understanding of their global distribution. This research has shown that in certain areas a small number of strains are causing a disproportionate number of cases of the disease. The sequencing of the complete genome of M tuberculosis has accelerated the development of molecular techniques to differentiate strains according to their genetic polymorphisms. Investigation into the reasons why some strains are predominant by genetic strain-typing techniques may clarify which bacterial factors contribute to disease. This knowledge has the potential to influence control and prevention strategies for tuberculosis in the future. However, there are still limitations in these techniques and their results. This review discusses molecular epidemiology and genetic studies, and their contribution to the understanding of the links between genotypic and phenotypic characteristics of M tuberculosis strains.</description><subject>Animals</subject><subject>Antitubercular Agents - therapeutic use</subject><subject>Bacterial diseases</subject><subject>Biological and medical sciences</subject><subject>Deoxyribonucleic acid</subject><subject>Disease</subject><subject>Disease control</subject><subject>DNA</subject><subject>DNA Fingerprinting</subject><subject>Drug resistance</subject><subject>Epidemiology</subject><subject>Gene sequencing</subject><subject>Genetic fingerprinting</subject><subject>Genetic variability</subject><subject>Genetic Variation</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Molecular chains</subject><subject>Molecular Epidemiology</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - classification</subject><subject>Mycobacterium tuberculosis - drug effects</subject><subject>Mycobacterium tuberculosis - genetics</subject><subject>Pathogenesis</subject><subject>Phenotypes</subject><subject>Phylogenetics</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Population Surveillance - methods</subject><subject>Strains (organisms)</subject><subject>Tuberculosis</subject><subject>Tuberculosis and atypical mycobacterial infections</subject><subject>Tuberculosis, Multidrug-Resistant - drug therapy</subject><subject>Tuberculosis, Multidrug-Resistant - genetics</subject><subject>Tuberculosis, Multidrug-Resistant - transmission</subject><issn>1473-3099</issn><issn>1474-4457</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqF0V1rFTEQBuAgiq3Vn6AsFkUvts1kd_NxJVJqFSq9aO_DbHaiKXt2j0m2cP69OR9QEKS5SRieGYa8jL0FfgYc5PkttKqpG27MJ9595tAAr-EZOy7ltm7bTj3fvffkiL1K6Z5zUMDbl-wIOiWl7MQxc5fek8upmn31iybKwVUPGAP2YQx5sy3_3Li5R5cphmVV5aWn6JZxTiFVKUcMU2meqvybqnWkRFPGHEqhdA4hESZ6zV54HBO9Odwn7O7b5d3F9_r65urHxdfr2nWc53pArYQW2EqtBZgeddM3TikwKIzyBrX3UrtecI-iB8fRS4mDk1yRF9ScsI_7ses4_1koZbsKydE44kTzkqxUHZhGigJP_4H38xKnspoVXBojoJyi3v9fgQTQXBfU7ZGLc0qRvF3HsMK4scDtNie7y8luQ7C8s7uc7Hb4u8PwpV_R8Nh1CKaADweAyeHoI04upEdXjDSqLe7L3lH52IdA0SYXaHI0hFhytcMcnljlL6wcrz0</recordid><startdate>20050301</startdate><enddate>20050301</enddate><creator>Malik, Aeesha NJ</creator><creator>Godfrey-Faussett, Peter</creator><general>Elsevier Ltd</general><general>Lancet Publishing Group</general><general>Elsevier Limited</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0TZ</scope><scope>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20050301</creationdate><title>Effects of genetic variability of Mycobacterium tuberculosis strains on the presentation of disease</title><author>Malik, Aeesha NJ ; Godfrey-Faussett, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c500t-da87282a4688219ba83b3c7719a297f9a8ff68cb20fa2b1c0af66adc607ef2e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Antitubercular Agents - 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Academic</collection><jtitle>The Lancet infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Malik, Aeesha NJ</au><au>Godfrey-Faussett, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of genetic variability of Mycobacterium tuberculosis strains on the presentation of disease</atitle><jtitle>The Lancet infectious diseases</jtitle><addtitle>Lancet Infect Dis</addtitle><date>2005-03-01</date><risdate>2005</risdate><volume>5</volume><issue>3</issue><spage>174</spage><epage>183</epage><pages>174-183</pages><issn>1473-3099</issn><eissn>1474-4457</eissn><coden>LANCAO</coden><abstract>The nature of the variability in the clinical and epidemiological consequences of Mycobacterium tuberculosis infection remains poorly understood. Environmental and host factors that contribute to the outcome of infection and disease presentation are well recognised, but the role of bacterial factors has been more elusive. The rapid increase in the understanding of the molecular basis of M tuberculosis over the past decades has revived research into its pathogenesis. DNA fingerprinting techniques have been used to distinguish between strains of M tuberculosis, and efforts to characterise the strains present within populations have led to increased understanding of their global distribution. This research has shown that in certain areas a small number of strains are causing a disproportionate number of cases of the disease. The sequencing of the complete genome of M tuberculosis has accelerated the development of molecular techniques to differentiate strains according to their genetic polymorphisms. Investigation into the reasons why some strains are predominant by genetic strain-typing techniques may clarify which bacterial factors contribute to disease. This knowledge has the potential to influence control and prevention strategies for tuberculosis in the future. However, there are still limitations in these techniques and their results. This review discusses molecular epidemiology and genetic studies, and their contribution to the understanding of the links between genotypic and phenotypic characteristics of M tuberculosis strains.</abstract><cop>London</cop><pub>Elsevier Ltd</pub><pmid>15766652</pmid><doi>10.1016/S1473-3099(05)01310-1</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Antitubercular Agents - therapeutic use Bacterial diseases Biological and medical sciences Deoxyribonucleic acid Disease Disease control DNA DNA Fingerprinting Drug resistance Epidemiology Gene sequencing Genetic fingerprinting Genetic variability Genetic Variation Genomes Genomics Human bacterial diseases Humans Infections Infectious diseases Medical sciences Mice Molecular chains Molecular Epidemiology Mycobacterium tuberculosis Mycobacterium tuberculosis - classification Mycobacterium tuberculosis - drug effects Mycobacterium tuberculosis - genetics Pathogenesis Phenotypes Phylogenetics Polymerase Chain Reaction Polymorphism, Restriction Fragment Length Population Surveillance - methods Strains (organisms) Tuberculosis Tuberculosis and atypical mycobacterial infections Tuberculosis, Multidrug-Resistant - drug therapy Tuberculosis, Multidrug-Resistant - genetics Tuberculosis, Multidrug-Resistant - transmission |
title | Effects of genetic variability of Mycobacterium tuberculosis strains on the presentation of disease |
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